AU2007209366A1

AU2007209366A1 - Use of hyaluronic acid as a carrier molecule for different classes of therapeutic active agents

Info

Publication number: AU2007209366A1
Application number: AU2007209366A
Authority: AU
Inventors: Massimo Bergamin; Susanna Bosi; Riaz Ahmed Khan; Erminio Murano; Stefano Norbedo
Original assignee: Eurand Pharmaceuticals Ltd
Current assignee: Allergan Pharmaceuticals Holdings Ireland ULC
Priority date: 2006-01-25
Filing date: 2007-01-25
Publication date: 2007-08-02
Also published as: IE20060049A1; WO2007085629A3; EP1976539A2; CA2640159A1; JP2009524624A; US20090197797A1; WO2007085629A2; CN101374531A

Description

WO 2007/085629 PCT/EP2007/050726 1 A NOVEL DRUG DELIVERY SYSTEM: USE OF HYALURONIC ACID AS A CARRIER MOLECULE FOR DIFFERENT CLASSES OF THERAPEUTIC ACTIVE AGENTS Prior art 5 Many drugs, which are hydrophobic in character and hence show poor solubility in water have been conjugated with hydrophilic polymers to increase their water solubility and improve the bioavailability. For this purpose a number polymeric materials showing the property of biocompatibility, biodegradability have been used, some of them are bioactive, have sufficient drug loading capacity, and have 1o drug targeting capabilities. Examples are polyglutamate, polyethylene glycole, carboxymethyl dextran and hyaluronic acid. However, PLG, PEG and CMD lack in bioactivity and targeting capabilities while HA has the advantage over the others because in addition it is bioactive and has the capability to target the drug to the diseased site. Many tumour types overexpress CD44 receptors; and HA can be 15 used to conjugate anticancer drugs to target the delivery of the drug to the diseased site. Endocytosis of derivatised HA has been shown in cell lines expressing CD44 HA receptor. The fluorescent labelled HA-Taxol conjugate has been shown to be selectively toxic towards human cancer cell lines which were known to overexpress HA receptors. The presence of liver receptors for HA 20 (HARLEC) suggests that it can be used as a carrier molecule to target a drug to the liver tissue. HA has been demonstrated for liver metastases from a colon adenocarcinoma in mice. The preparation of HA substituted at the C-6 primary hydroxyl group with dihydrofolate reductase inhibitors (DHFR) have been described in WO0168105. 25 This conjugate has been obtained by preparing HA-6-halogen by selective halogenation reaction of HA, and followed by displacement of the halogen by the DHFR. This conjugate is still endowed with antiproliferative activity, however it still presents the problem that it contains residual halogen groups. Selective introduction of a leaving group on polysaccharide has been described in 30 Carb. Res. 340, 2229-2235, 2005 where a tosylation of cellulose in a mixture of acetamide and lithium chloride is reported; the conditions chosen allows the WO 2007/085629 PCT/EP2007/050726 2 complete sulfonylation of all the primary hydroxyl groups with the aim of blocking said positions and introducing other chemical groups on the free positions. Description of the figures FIGURE 1: represents the formula of DDSs: HA-6-methotrexate, HA-6-ibuprofen, 5 HA-6-PenG FIGURE 2: represents the DOSY NMR spectrum of HA-6-OMs obtained in example 9 (in DOSY weighed monodimensional NMR spectra only rigid macromolecules are present, furnishing evidence for polymer chemical modification) 10 FIGURE 3: represent the 13C NMR spectrum of HA-6-OMs, peaks of salifying DIEA are present. FIGURE 4: represents the DOSY NMR spectrum of HA-6-MTX obtained in example 24 FIGURE 5: represents the 13C NMR spectrum of HA-6-MTX obtained in example 15 24 FIGURE 6: represents the DOSY NMR spectrum of HA-Ibuprofen obtained in example 26 FIGURE 7: represents the 13C NMR spectrum of HA-Ibuprofen obtained in example 26 20 FIGURE 8: represents the DOSY NMR spectrum of HA-Penicillin G obtained in example 29 Detailed description of the invention In a first aspect of the invention, there is provided a drug delivery system (DDS) consisting of hyaluronic acid (HA) and a therapeutic active agent, whereby this 25 active agent is covalently linked at the C-6 position of the N-acetyl-D-glucosamine residue of the hyaluronic acid with the exception of active agents of formula (I): 30 WO 2007/085629 PCT/EP2007/050726 3 R4 ICOOH I N( CH 2 - Z - Ar - CONH - CH - (CH 2

)

2 -7 COOH R2 formula (I) wherein:

R

2 and R 4 independent from one another represent: -NH 2 , -OH, -OCH 3 , 01-05 alkyl, =0; X and Y represent: -C(R 5 )=, -CH(R 5 )-, -NH-, -N=) , wherein R 5 5 represents: -H, C1-C5 alkyl; Z represents: -CH(Rio)-, -N(Rio)-, -0-; R i o represents: -H, Ci-C5 alkyl, Ci-C5 alkenyl, Ci-C5 alkynyl, 5-6 membered heterocyclic ring with 1-3 heteroatoms selected in the group consisting of nitrogen, sulphur and oxygen; Ar represents: 1,4-phenyl group, 1,4-phenyl group condensed with one or more 5 6 membered aromatic rings, 1,4-phenyl group condensed with one or more 5-6 10 membered heterocycles, wherein said Ar is possibly substituted with R 2 ; rings A and b, independently from one another, may be aromatic or non-aromatic. The compounds of formula (1) are the dihydrofolato reductase inhibitors described in WO0168105. Hyaluronic acid (also herein indicated as HA) is composed of a disaccharidic 15 repeating unit, consisting of D-glucuronic acid and 2-acetamido-2-deoxy-D-glucose (N-acetyl-D-glucosamine) bound by 3(1-> 3) glycosidic linkage; the D-glucuronic acid residue may either be in the acid form or in the form of a salt. Each repeating unit is bound to the next one by a 3(1->4) glycosidic linkage that forms a linear polymer. 20 The term hyaluronic acid, as used in the present invention, encompasses both the acid and the salified form. The term hyaluronic acid is commonly used to describe a general group of molecular fractions of HA with varying molecular weights or also hydrolysed fractions of said compound. For the purposes of the present invention the WO 2007/085629 PCT/EP2007/050726 4 hyaluronic acid has preferably an average molecular weight comprised between 10000 to 1 million and more preferably 20000 to 500000. The therapeutic active agent is chosen from drugs belonging to a number of different therapeutic categories: analgesic, antihypertensive, anestetic, diuretic, 5 bronchodilator, calcium channel blocker, cholinergic, CNS agent, estrogen, immunomodulator, immunosuppressant, lipotropic, anxiolytic, antiulcerative, antiarrhytmic, antianginal, antibiotic, anti-inflammatory, antiviral, thrombolitic, vasodilator, antipyretic, antidepressant, antipsychotic, antitumour, mucolytic, narcotic antagonist, hormones, anticonvulsant, antihistaminic, antifungal, 10 antipsoriatic. These therapeutic active agents contain a nucleophilic group. A nucleophilic group is an electron-pair donor group such as carboxylic, amino, substituted amino, hydroxyl, thiol, amide group; the carboxylic group is preferred. In the DDS the linkage between the hyaluronic acid and the active agent is an 15 ester, an amino, an ether, a thioether, an amide. The ester linkage is preferred. The DDSs are either in the acid form or in the salt form. When they are in salt form they may be salified with alkaline metals (preferably Na or K), earth-alkaline metals (preferably Ca or Mg), transition metals (preferably Cu, Zn, Ag, Au, Co, Ag). The salification is obtained by processes known by the skilled artisan. 20 Optionally, also the secondary hydroxyl groups on the DDSs may be derivatised to form a group selected from: -OR, -OCOR, -SO 2 H, -OPO 3

H

2 , -O-CO-(CH 2 )n-COOH,

-O-(CH

2 )n-OCOR, wherein n is 1-4 and R is C1-Clo0 alkyl, -NH 2 , -NHCOCH 3 .These substitutions can be easily obtained by processes known in the art, and they may be chosen in order to modulate the hydrophilic character of the DDSs. 25 The total amount of the therapeutic active agent in the DDSs is defined by the degree of substitution (C6-DS); the latter can alternatively indicate the % by weight of the active agent with respect to the total weight of the DDS (C6-DSw) or the % by mole of the active agent with respect to the mole of repeating unit of modified HA (C6-DSmol). 30 In the DDS of the invention the C6-DSw is preferably comprised between 0.1 and 60%, more preferably between 1 and 50%, even more preferably between 5 and 40%.

WO 2007/085629 PCT/EP2007/050726 5 As demonstrated in the experimental part, the invented DDSs are characterised by the presence of active agent directly linked to the primary hydroxyl groups of the N-acetyl-D-glucosamine units of the hyaluronic acid. No other hydroxyl groups of 5 the HA are involved in the chemical linkage with the drug. Moreover, the DDSs are stable and free of undesired reaction by-products and impurities that can be harmful to their practical pharmaceutical use. They retain the pharmaceutical effect of the therapeutic agent. Therefore, they can be successfully used in the treatment of all pathologies that are appropriate for the 10 specific therapeutic active agent in the DDS. Accordingly, it is a further aspect of the invention the use of the above DDSs in the manufacture of a medicament for the treatment of pathologies appropriate for each therapeutic agent. Said pathologies are selected from the group consisting of tumours, skin disorders, psoriasis, inflammatory pathologies, rheumatoid arthritis, 15 and infectious diseases. It is also an aspect of the invention a pharmaceutical composition containing the DDSs of the invention in admixture with pharmaceutically acceptable excipients and/or diluents. The pharmaceutical composition may be either in the liquid or in solid form; it may be administered through the oral, parenteral, topical route. 20 Particularly interesting are the injectable pharmaceutical compositions containing the invented DDSs. A further aspect of the invention is a technology for the preparation of the drug delivery system of HA and a therapeutic active agent with the exception of compounds of formula (I) having the features described above. It has been 25 surprisingly found that the reaction does not only occurs with compound having the structure of formula (I) having two carboxylic groups and heterocyclic rings, but this process is widely applicable to a high number of different active agents which belong to different therapeutic categories. This technology comprises the following reaction steps: 30 (a) introducing a leaving group at the C-6 position of the N-acetyl-D-glucosamine units of the hyaluronic acid either in the free form or in the salt form thus obtaining a HA-6-activated WO 2007/085629 PCT/EP2007/050726 6 (b) forming a chemical linkage between the C6 position of the HA-6-activated and the therapeutic active agent by displacing the leaving group (at the C6 position of HA) with a nucleophilic group present on the therapeutic active agent, thereby obtaining a HA-6-active agent 5 (c) possible displacing of any un-substituted leaving group from the HA-6-active agent obtained in step (b) (d) recovering the HA-6-active agent With this process it is possible to obtain DDSs having a C6-DSw preferably comprised between 0.1 and 60%, more preferably between 1 and 50%, and even 10 more preferably between 5 and 40%. There are two different ways of carrying out the process of the invention. In a first way the HA-6-activated obtained from step (a) is isolated from the reaction mixture and then reacted with the therapeutic active agent according to step (b) to give the final HA-6-active agent that may optionally undergo step (c). 15 In the second way of carrying out the process, the step (b) is performed directly on the reaction mixture obtained in step (a) that contains the HA-6-activated. The advantage of this second way of performing the reaction consists in the fact that the isolation step of the HA-6-activated is avoided. The starting HA may be in free form or in the form of salt, wherein the counterion 20 is preferably an alkaline or alkaline-earth metal or is a nitrogen-containing counterion. In the latter case the counterion may contain heterocycles selected from the group consisting of pyridine, pyrazine, pyrimidine, pyrrole, pyrazole, imidazole triazole, tetrazole, possibly substituted with one or more C1-C6 alkyl groups. Preferred examples of nitrogen-containing counterions are ammonium, 25 tetrabutylammonium (TBA), pyridinium or sym-collidinium ions. Step (a) is a selective reaction carried out by adding the suitable reagent to a thoroughly stirred suspension or solution of HA (in free form or in the salified form) in an aprotic organic solvent. The leaving group which is introduced at the C-6 position of the glucosamine unit 30 of the HA is any electron-pair acceptor group that departs during the substitution by a nucleophile group. It may be selected from the group consisting of sulfonate group, phosphonate group (triphenylphoshonate), cyanide (CN-), nitrite (NO2-), WO 2007/085629 PCT/EP2007/050726 7 halogen (preferably chloro), sulphate group, halogensulfate group, nitrate, halogensulfite (chlorosulfite). When the leaving group is halogen the halogenation is carried out as described in WO9918133 and WO0168105. Among the halogen group the chlorine group is the 5 preferred one and the preferred reagent to perform the halogenation is methanesulfonyl chloride in N,N-dimethylformamide. This step allows the formation of the HA-6-activated. Step (b) is performed by reacting the hyaluronic acid-6-activated or one of its salt obtained form step (a) with the therapeutic active agent. It consists in the 1o substitution of the leaving group by the nucleophilic group contained in the active agent and entails the formation of a covalent linkage between the C-6 position of hA and the active agent. The chemical nature of said linkage depends on the chemical nature of nucleophile group. It may be an ester linkage which is formed when the nucleophile is a carboxylic group. Other linkages that are formed 15 between the HA and the therapeutic active agent are: amino, ether, thioether, amide. Step (c) is a possible step that may be any suitable reaction that allows the displacement of any possible un-substituted leaving group. Such a displacement may be carried out for example by photolyisis, by reduction. In some case, step (c) 20 is not necessary since some un-substituted leaving group may be destroyed during the step (b) either because of the reaction conditions or during the work-up. In step (d) the obtained the HA-6-active agent (DDS) is recovered by means of standard techniques. In a preferred embodiment of the process the leaving group is the sulfonyl group 25 and the obtained activated HA is therefore HA-6-sulfonated. This preferred reaction comprises the following reaction steps: (a) introducing a sulfonate group at the C-6 position of the N-acetyl-D-glucosamine units of the hyaluronic acid in the salt form thus obtaining a HA-6-sulfonated (b) forming a chemical linkage between the C-6 position of the HA-6-sulfonated 30 and the therapeutic active agent by displacing the sulfonated group (at the C-6 position of HA) with the nucleophilic group present on the therapeutic active agent, thereby obtaining a HA-6-active agent.

WO 2007/085629 PCT/EP2007/050726 8 (d) recovering the HA-6-active agent In this embodiment, the selective sulfonylation reaction of step (a) is carried out using as sulfonylating reagent an alkyl- or aryl-sulfonyl halide, preferably chloride, 5 in presence of an organic or inorganic base, preferably an organic base. The alkyl or aryl-sulfonyl halide may be chosen among, preferred are methylsulfonyl (mesyl), toluene-p-sulfonyl (tosyl), trifyl, trimsyl, tripsyl, 1,1-sulfonyl-imidazole. The organic base is selected preferably among the different organic amines, such as diisopropylethylamine, triethylamine. 10 The solvent is chosen from the group consisting of: dimethylformamide, dimethylacetamide, dimethylsulfoxide, formamide. The general sulfonylation procedure is as follows. The base, preferably organic base is added to a suspension or a solution of HA in salt form, preferably in an organic base form, by stirring under nitrogen flux. Then the alkyl- or aryl-sulfonyl 15 chloride in a suitable solvent, preferably the same solvent, is added dropwise. After a period of time ranging from 2 to 90 minutes (preferably 45-75 min), the reaction is quenched by addition of NaHCO3 to remove the formate ester groups formed during the reaction at secondary hydroxyl groups of HA. Then the reaction is allowed to continue for about 10-20 hours, preferably 18 hours. The reaction 20 product (HA-6-sulfonated) is either directly recovered form the solution by means of known techniques, such as precipitation, drying or before recovery the solution is treated in such a way as to allow the obtainement of the HA-6-sulfonated in a suitable salt form, such as HA-6-sulfonated:TBA. The reaction conditions are mild; in fact, reaction can be successfully carried out at 25 room temperature or at a lower temperature, no cooling-heating cycles are required, pH conditions are mild. The reagent is used in limited quantities, the suitable amount is 1-10 molar equivalents with respect to the repeating HA unit (preferably 2-6 molar eq) of sulfonyl halide (such as mesylchloride), in the presence of 2-20 molar equivalents 30 with respect to the repeating HA unit (preferably 4-12 molar eq) of organic amine (such as DIEA).

WO 2007/085629 PCT/EP2007/050726 9 Under the above reaction conditions the obtained hyaluronic acid-6-sulfonated has degree of substitution (DSmo), ranging from 10% to 91% mol/mol, preferably from 20 to 90%, even more preferably from 40 to 80%. The selectivity of the mesylation reaction for the primary position (C-6) of the N-acetyl-D-glucosamine residue is 5 between 50 and 100% (C6-DSmol). Some mesylation reactions also occurs at the secondary positions, such as at C-4 of N-acetyl-D-glucosamine and at the C-2, C-3 positions of the D-glucuronic acid residue. Their structures and the degree of mesyl group substitution in the polymer are confirmed by NMR spectroscopy. In a preferred embodiment of the sulfonylation reaction, step (b) entails the 1o formation of an ester linkages group between the HA and the carboxylic group present on the therapeutic agent. In this last embodiment, step (a) is carried out as described above and step (b) is usually performed according to the following procedure. A solution of the carboxylic group containing-active agent is added to a solution of 15 the HA-6-sulfonated either in TBA or in the sodium salt form, preferably TBA, in presence of an alkaline or alkaline-earth metal salt, such as cesium carbonate. The reaction is carried out between 40-90oC, preferably 800C under constant stirring, preferably under nitrogen flux for a period of time ranging form 5 to 42 hours, preferably form 8 to 20 hours (18 hours). The reaction mixture is worked up 20 according to known techniques. A further aspect of the present invention is a drug delivery system consisting of hyaluronic acid and a compound of formula (I), whereby the carboxylic group of compound of formula (I) is covalently linked at the C-6 position of the N-acetyl-D glucosamine units of the hyaluronic acid by means of an ester linkage and said 25 DDS is obtained by the specific process described hereunder. These new DDSs contain the compound of formula (I) directly linked at the C-6 position of the HA and are characterised by the fact and no other hydroxyl groups of the HA repeating unit is involved in chemical linkage neither with the drug nor with other chemical groups. In particular these DDSs are devoid of any residual leaving 30 groups (such as sulfonate group) both on the primary and on the secondary positions of the HA units. The term "devoid" means that the residual leaving group is present in an amount below 0.5% w/w as determined by NMR. These features WO 2007/085629 PCT/EP2007/050726 10 allows the maintenance of the regularity of the original HA chemical structure and the retention of the configuration of the carbon atoms, these properties/aspects are highly important to ensure the efficacy and the interaction with the specific receptors. 5 Differently, the conjugate of HA and methotrexate that was described in WO0168105 contains residual chlorine atoms, that are introduced on the polysaccharide during the halogenation step. Among the different compounds having formula (I) the preferred one is methotrexate. Methotrexate (MTX) is represented by formula (I) where R 2 and R 4 10 are -NH 2 ; ring A is aromatic; ring B is aromatic; X and Y are: -N=; Z is: -N(CH3)-; Ar is: 1,4-phenyl group. The C6-DSw of the DDSs is preferably comprised between 0.1 and 60%, more preferably between 1 and 50%., even more preferably between 5 and 40%, the MW is comprised between 10,000 and 500,000. The technology for the preparation of this DDS comprises the following reaction 15 steps: (a) introducing at the C-6 position of the N-acetyl-D-glucosamine units of the hyaluronic acid either in the free form or in the salt form a leaving group selected from the group consisting of sulfonate group, phosphonate group (triphenylphoshonate), cyanide (CN-), nitrite (N02-), sulphate group, 20 halogensulfate group, nitrate, halogensulfite (chlorosulfite) thus obtaining a HA-6 activated (b) forming an ester linkage between the C6 position of the HA-6-activated and the compound of formula (I) by displacing the leaving group (at the C6 position of HA) with a carboxylic group present on compound (I), thereby obtaining a HA-6 25 compound of formula (I) (d) recovering the HA-6- compound of formula (I) In the preferred embodiment, step (a) is a sulfonylation reaction and the reagent used for introducing the sulfonate group is an alkyl- or aryl-sulfonyl halide, preferably chloride, in presence of an organic or inorganic base. The preferred the 30 reagent is methylsulfonyl chloride or toluene-p-sulfonyl chloride and the organic base is diisopropylethylamine or triethylamine.

WO 2007/085629 PCT/EP2007/050726 11 The DDS can be obtained with the above process according to two different ways. In the first way the HA-6-sulfonated obtained from step (a) is isolated from the reaction mixture and then reacted with the compound of formula (I) according to step (b) to give the final HA-6-compound of formula (I). 5 In the second way of carrying out the process, the step (b) is performed directly on the reaction mixture obtained in step (a) that contains the HA-6-sulfonated. The advantage of this second way of performing the reaction consists in the fact that the isolation step of the HA-6-sulfonated is avoided. EXPERIMENTAL PART 10 EXAMPLE 1: Determination of structure The determination of mesylate content in the HA-6-Mesylate (HA-Ms) by NMR was achieved by integration of the peaks in the region 3.10+3.32ppm (1H of HA chain and 3H of mesylate) versus the peak at 1.95ppm (3H of HA chain). EXAMPLE 2: Determination of structure 15 The determination of tosylate content in the HA-6-tosylate (HA-Ts) by NMR was achieved by integration of the peaks of tosylate at 7.8ppm (2H), 7.5ppm (2H) and 2.45ppm (3H) versus the peak at 1.95ppm (3H of HA chain). EXAMPLE 3: Determination of structure Determination of methotrexate content in HA-6-MTX by NMR was achieved by 20 integration of the peaks in the region 6.0+8.6ppm (5H of MTX) versus the peaks in the region 1.85+2.58ppm (3H of HA chain and 4H of MTX). EXAMPLE 4: Determination of structure The determination of Ibuprofen in HA-6-lbuprofen by NMR was achieved by integration of the peaks of ibuprofen in the regions 7.02+7.24ppm (4H), 2.38ppm 25 (2H), 1.40ppm (3H), 0.78ppm (6H) versus the peak of the HA chain at 1.95ppm (3H). EXAMPLE 5: Determination of structure The determination of Penicillin G in HA-6-Penicillin G by NMR was achieved by integration of the peaks of Penicillin G in the regions 7.05+7.20ppm (5H), 5.55ppm 30 (1 H), 5.40 (1 H) versus the peak of the HA chain at 1.95ppm (3H).

WO 2007/085629 PCT/EP2007/050726 12 EXAMPLE 6: Methotrexate content by HPLC was determined by analysing the samples before and after alkaline hydrolysis according to Methotrexate Official Monograph (USP 23-p 984). The analyses conditions were: Cromatograph: Dionex DX-600. Column: Column Phenomenex Synergi 4p Hydro-RP80, Column 5 size:150X460mm, Column particle size : 4p, Temperature: 40 0 C Eluent: 90% 0.2M dibasic sodium posphate/0.1M citric acid (630:270), 10% CH 3 CN, isocratic condition: 0.5 mL/min. Detector: Diode Array (range 200-780nm), Selected wavelength for the quantitative determination: 302 nm Injected volume:25 [[l, run time 30 minutes. Solutions for free methotrexate determination were prepared by 10 dissolving HA-MTX directly in MilliQ water at the appropriate concentration. Total methotrexate content was determined after alkaline hydrolysis carried out in NaOH 0.1 M, room temperature for 2 hours. After neutralization with hydrochloric acid 1 M, solutions were filtered through 0.45 pIm (Sartorius Minisart RC25 17795Q) prior to injection in the HPLC system. A calibration curve was determined by using 15 standard solutions with known concentration of methotrexate. The method gives the MTX concentration in the sample solution, which normalized by the sample concentration yields the DSweight %W/W. EXAMPLE 7: Determination of weight average molecular weight (Mw). The molecular weight of the hyaluronic acid DDS was measured by HP-SEC (High 20 Performance Size Exclusion Chromatography). The analysis conditions were: Chromatograph: HPLC pump 980-PU (Jasco Ser. No. B3901325) with Rheodyne 9125 injector. Column: TSK PWxl (TosoBioscience) G6000+G5000+G3000 6, 10, 13 pIm particle size; Temperature: 40 0 C Mobile phase: NaCI 0.15 M + 0.01% NaN 3 . Flux: 0.8 mL/min. Detector: MALS (WYATT DAWN EOS - WYATT, USA), 25 X= 690 nm, (dn/dc = 0.167 mL/g), UV spectrophotometric detector 875-UV (Jasco, Ser. No. D3693916), A = 305 nm, Interferometric Refractive Index OPTILAB REX (WYATT, USA); X=690 nm, Sensitivity: 128x; Temperature: 35 0 C Injected volume:100 [[l, run time 60 minutes. The samples of HA-CI, HA-OMs, HA-MTX, HA-conjugated to different drugs to be 30 analysed were solubilised in 0.9 % NaCI at the concentration of about 1.0 mg/ml and kept under stirring for 12 hours. Then, the solutions were filtered on a 0.45 tm porosity filter (Sartorius Minisart RC25 17795Q) and finally injected in the WO 2007/085629 PCT/EP2007/050726 13 chromatograph. The analysis allows the measurement of Mw (weight average molecular weight), Mn (number average molecular weight), PI (polydispersity). Mw and Mn values are expressed as g/mole.The concentration of the polymeric samples solutions were controlled by means of the integral of the refractive index. 5 EXAMPLE 8: Preparation of 6-O-Methanesulfonylhyaluronic acid (HA-6-Ms or HA MS) To a solution of 500 mg (0.806 mmol) of TBA salt of HA (MW 20,000) in 20 ml of dimethylsulfoxide (DMSO) were added 1.11ml (6.48mmol) of diisopropylethylamine (DIEA) by stirring under nitrogen. Methanesulfonyl chloride 10 (MsCI) (314pL; 4.03mmol) was then added dropwise at room temperature, whereupon an orange solution formed. After 1 h stirring at room temperature, one third of the reaction mixture was quenched by pouring into saturated NaHCO 3 solution (50ml), stirring overnight at pH 9. The resulting solution was ultrafiltered, concentrated in a rotary evaporator and freeze-dried to afford 40mg of an off-white 15 solid (total DS 83% mol/mol by NMR). The rest of the reaction mixture was stirred overnight and then worked up as described above, to obtain 90mg of an off-white solid (total DS 86% mol/mol by NMR). Overall yield: 130mg of HA-Ms sodium salt (40%). 20 1 H NMR (D 2 0) ppm: 1.95 (s, 3H, NHCOCH 3 ), 3.23 (s, 2.58H, MsO), 3.2+4.2 (m, 7.42H, HA chain), 4.3+4.7 (m, 2H, anomeric + 1.72H, CH-OMs); 13C NMR (D 2 0) ppm: 23 (NHCOCH 3 ), 37 (MsO), 55, 61 (CH 2 OH), 68, 69.5 (CH 2 OMs), 72, 74, 75, 76, 80, 83, 101, 103, 174,175. EXAMPLE 9: Preparation of 6-O-Methanesulfonylhyaluronic acid (HA-Ms) 25 To a solution of 5.00 g (8.06 mmol) of TBA salt of HA (MW 20,000) in 200 ml of DMSO were added 13.9ml (81 mmol) of DIEA by stirring under nitrogen. MsCI (3.2 ml; 41mmol) was then added dropwise at room temperature, whereupon an orange solution was formed. After 1 h stirring at room temperature, the reaction mixture was quenched by pouring into saturated NaHCO 3 solution (400 ml), 30 bringing the total volume to 1L with water (resulting pH: 9.5) and maintaining stirring overnight. The resulting solution was ultrafiltered under a hood and concentrated in a rotary evaporator. A small portion was evaporated to dryness in WO 2007/085629 PCT/EP2007/050726 14 a rotary evaporator (100 mg) for NMR analysis: total mesylate DS 91% mol/mol by proton NMR, primary mesylates 58% mol/mol by carbon NMR, selectivity 64% for the C6 position. The rest of the solution was treated with amberlite IRA-120 loaded with TBA and 5 freeze-dried to afford 4.62g of an off-white solid (HA-Ms:TBA salt). EXAMPLE 10: Preparation of 6-O-Methanesulfonylhyaluronic acid (HA-Ms) To a solution of 2.50 g (4.03 mmol) of TBA salt of HA (MW 20,000) in 100 ml of DMSO were added 5.6 ml (32.7mmol) of DIEA by stirring under nitrogen. MsCI (1.3 ml; 16.7mmol) was then added dropwise at room temperature, whereupon an 10 orange solution was formed. After 1 h stirring at room temperature, the reaction mixture was quenched by pouring into saturated NaHCO 3 solution (200 ml), bringing the total volume to 600ml with water (resulting pH: 9.2), and maintaining stirring overnight. The resulting solution was ultrafiltered under a hood and concentrated in a rotary evaporator. A small portion was freeze-dried (136mg) for 15 NMR analysis: total mesylate DS 79% mol/mol by proton NMR, primary mesylates 64% mol/mol by carbon NMR, selectivity 81% for C6 position. The rest of the solution was treated with amberlite IRA-120 loaded with TBA and freeze-dried to afford 2.10Og of an off-white solid (HA-Ms:TBA salt). EXAMPLE 11: Preparation of 6-O-Methanesulfonylhyaluronic acid (HA-Ms) 20 To a solution of 3.00 g (4.84 mmol) of TBA salt of HA (MW 20,000) in 100 ml of DMSO were added 8.4 ml (48.4 mmol) of DIEA by stirring under nitrogen. MsCI (1.92 ml; 24.2 mmol) was then added dropwise at room temperature, whereupon an orange solution formed. After 15min stirring at room temperature, the reaction mixture was quenched by pouring into saturated NaHCO 3 solution (200ml), 25 bringing the total volume to 600ml with water (resulting pH: 9.5) and maintaining stirring overnight. The resulting solution was ultrafiltered under a hood and concentrated in a rotary evaporator. A small portion was freeze-dryed (187mg) for NMR analysis: total mesylate DS 76% mol/mol by proton NMR, primary mesylates 58% mol/mol by carbon NMR, selectivity 76% for C6. 30 The rest of the solution was treated with amberlite IRA-120 loaded with TBA and freeze-dried to afford 2.561g of an off-white solid (HA-Ms:TBA salt).

WO 2007/085629 PCT/EP2007/050726 15 EXAMPLE 12: Preparation of 6-O-Methanesulfonylhyaluronic acid (HA-Ms) To a solution of 3.00g (4.84mmol) of HA TBA salt (MW 20.000) in DMSO (100 ml) were added 4.96ml (29.0mmol) of DIEA by stirring under nitrogen. MsCI (1.13ml; 14.5mmol) was then added dropwise at room temperature, whereupon an orange 5 solution was formed. After 15min stirring at room temperature, the reaction mixture was quenched by pouring into saturated NaHCO 3 solution (200ml), bringing the total volume to 600ml with water (resulting pH: 9.5) and maintaining stirring overnight. The resulting solution was ultrafiltered under a hood and concentrated in a rotary evaporator. A small portion was freeze-dried (248mg) for NMR analysis: 10 total mesylate DS 55% mol/mol by proton NMR, primary mesylates 41% mol/mol by carbon NMR, selectivity 75% for C6. The rest of the solution was treated with amberlite IRA-120 loaded with TBA and freeze-dried to afford 2.41 g of an off-white solid (HA-Ms:TBA salt). EXAMPLE 13: Preparation of 6-O-Methanesulfonylhyaluronic acid (HA-Ms) 15 To a solution of 3.00g (4.84mmol) of HA TBA salt (MW 20.000) in DMSO (100 ml) was added DIEA (4.96ml; 29.0mmol) by stirring under nitrogen. MsCI (1.13ml; 14.5mmol) in dichloromethane (20ml) was then added dropwise during 20 min, at room temperature, whereupon an orange solution formed. The reaction mixture was then immediately quenched by pouring into saturated NaHCO 3 solution 20 (200ml), bringing the total volume to 600ml with water (resulting pH: 9.5) and maintaining stirring overnight. The resulting solution was ultrafiltered under a hood and concentrated in a rotary evaporator. A small portion was freeze-dried (172mg) for NMR analysis: total mesylate DS 85% mol/mol by proton NMR, primary mesylates 50% mol/mol by carbon NMR, selectivity 59% for C6. 25 The rest of the solution was treated with amberlite IRA-120 loaded with TBA and freeze-dried to afford 2.78g of an off-white solid (HA-Ms:TBA salt). EXAMPLE 14: Preparation of 6-O-Methanesulfonylhyaluronic acid (HA-Ms) To a suspension of 3.00g (7.48mmol) of HA sodium salt (MW 20.000) in DMSO (100ml) were added DIEA (12.8ml; 74.8mmol) and MsCI (2.90ml; 37.4mmol), 30 observing the formation of a dark orange colour within one minute. After lh and 15min stirring at room temperature, the reaction mixture was quenched by pouring into saturated NaHCO 3 solution (200ml), bringing the total volume to 800ml with WO 2007/085629 PCT/EP2007/050726 16 water (resulting pH: 9.5) and maintaining stirring overnight. The resulting solution was ultrafiltered under a hood and concentrated in a rotary evaporator. A small portion was freeze-dried (0.15g) for NMR analysis: total mesylate DS 5% mol/mol by proton NMR. 5 EXAMPLE 15: Preparation of 6-O-p-toluenesulfonylhyaluronic acid A solution of HA:TBA salt (1.018 g; 1.64 mmol) (MW 20000) in 30ml of dry DMF was treated with Et 3 N (3.2 mL; 23.0 mmol) and TsCI (2.24 g; 11.7 mmol) at room temperature; the reaction mixture turned orange-red and the solution became viscous. After 1hour, 6ml of the reaction mixture was concentrated to half volume 10 in a rotary evaporator and the sample was precipitated with acetone. A little amount of solid was dissolved in DMSO-d 6 and 1 H NMR and DOSY NMR spectra were obtained, which showed that the DS of the tosyl group was 16% mol/mol; 95 mg of the formylated sample were recovered. 1 H NMR (d 6 -DMSO) ppm: 1.95 (s, 3H, NHCOCH 3 ), 2.45 (s, 0.49H, tosylate CH 3 ), 15 3.0+5.4 (m, 12.3H, HA chain and anomeric), 7.5 (d, 0.34H, tosylate aromatics), 7.85 (d, 0.30H, tosylate aromatics), 8.0+8.5 (m, 2.14H, O-CHO formyl ester groups). The rest of the reaction was heated to 500C for a further hour, quenched in a saturated NaHCO 3 solution at pH 9, stirred for 24 hours, neutralised and filtered to 20 remove solids. Than the solution was ultrafiltered and freeze-dried. 1 H NMR and DOSY NMR spectra in DMSO-d 6 were obtained, which showed that the DS of the tosyl group was 12% mol/mol. 55 mg of sample were recovered. EXAMPLE 16: Preparation of 6-O-p-toluenesulfonylhyaluronic acid A solution of HA:TBA salt (1.053 g; 1.70 mmol) (MW 20000) in 30ml of dry DMF 25 was treated with Et 3 N (3.2 mL; 23.0 mmol) and TsCI (2.24 g; 11.7 mmol) at 0oC; the reaction mixture turned orange-red and the solution became viscous. After 30 minutes, It was then brought to room temperature and after a further hour, the reaction mixture was concentrated to half volume in a rotary evaporator and the sample was precipitated with acetone. A little amount of solid was dissolved in 30 DMSO-d 6 and 1 H NMR and DOSY NMR spectra were obtained, which showed that the DS of the tosyl group was 45% mol/mol; 700 mg of the formylated sample were recovered.

WO 2007/085629 PCT/EP2007/050726 17 1 H NMR (d 6 -DMSO) ppm: 1.95 (s, 3H, NHCOCH 3 ), 2.45 (s, 1.36H, tosylate CH 3 ), 3.0+5.4 (m, 13.0H, HA chain and anomeric), 7.5 (d, 0.97H, tosylate aromatics), 7.85 (d, 0.90H, tosylate aromatics), 8.0+8.5 (m, 2.33H, O-CHO formyl ester groups) 5 EXAMPLE: 17 Preparation of 6-O-Methanesulfonylhyaluronic acid (HA-Ms) To a solution of 500mg (0.806mmol) of TBA salt of HA (MW 20,000) in 20 ml of DMSO were added 829pL (4.84mmol) of DIEA by stirring under nitrogen. MsCI (188pL; 2.42mmol) was then added dropwise at room temperature, whereupon an orange solution was formed. After 1 h stirring at room temperature, the reaction 1o mixture was quenched by pouring into saturated NaHCO 3 solution (40ml), bringing the total volume to 100ml with water (resulting pH: 9.5) and maintaining stirring overnight. The resulting solution was ultrafiltered under a hood and concentrated in a rotary evaporator. The solution was freeze-dried to afford 329mg of a white solid. Total mesylate DS 77% mol/mol by proton NMR, primary mesylates 59% 15 mol/mol by carbon NMR, selectivity 77% for the C6 position. EXAMPLE 18: Preparation of 6-O-Methanesulfonylhyaluronic acid (HA-Ms) To a solution of 500mg (0.806mmol) of TBA salt of HA (MW 20,000) in 20 ml of DMSO were added 414pL (2.42mmol) of DIEA by stirring under nitrogen. MsCI (94pL; 1.21mmol) was then added dropwise at room temperature, whereupon an 20 orange solution was formed. After 1 h stirring at room temperature, the reaction mixture was quenched by pouring into saturated NaHCO 3 solution (40ml), bringing the total volume to 100ml with water (resulting pH: 9.5) and maintaining stirring overnight. The resulting solution was ultrafiltered under a hood and concentrated in a rotary evaporator. The solution was freeze-dried to afford 310mg of a white 25 solid. Total mesylate DS 34% mol/mol by proton NMR, primary mesylates 22% mol/mol by carbon NMR, selectivity 65% for the C6 position. EXAMPLE 19: Preparation of 6-O-Methanesulfonylhyaluronic acid (HA-Ms) To a solution of 500mg (0.806mmol) of TBA salt of HA (MW 20,000) in 20 ml of DMF were added 829pL (4.84mmol) of DIEA by stirring under nitrogen. MsCI 30 (188pL; 2.42mmol) was then added dropwise at room temperature, whereupon a yellow solution was formed. After 1 h stirring at room temperature, the reaction mixture was quenched by adding saturated NaHCO 3 solution (40ml) and bringing WO 2007/085629 PCT/EP2007/050726 18 the total volume to 100ml with water (resulting pH: 9.5); stirring was maintained overnight. The pH was raised to 10 and the suspension was stirred for 3 days, whereupon most of the solids dissolved. Then it was filtered and the resulting solution was ultrafiltered and concentrated in a rotary evaporator. The solution was 5 freeze-dried to afford 277mg of a white solid. Total mesylate DS 42% mol/mol by proton NMR, primary mesylates 40% mol/mol by carbon NMR, selectivity 95% for the C6 position. EXAMPLE 20: Preparation of 6-O-Methanesulfonylhyaluronic acid (HA-Ms) To a solution of 500mg (0.806mmol) of TBA salt of HA (MW 20,000) in 20 ml of 10 DMF were added 829pL (4.84mmol) of DIEA by stirring under nitrogen at -10oC. MsCI (188pL; 2.42mmol) was then added dropwise and the resulting mixture was stirred for l1h at -10oC. The reaction mixture was quenched by adding saturated NaHCO 3 solution (40ml) and bringing the total volume to 100ml with water (resulting pH: 9.5); stirring was maintained overnight. The resulting solution was 15 ultrafiltered and concentrated in a rotary evaporator. The solution was freeze-dried to afford 207mg of a white solid. Total mesylate DS 37% mol/mol by proton NMR, primary mesylates 37% mol/mol by carbon NMR, selectivity 100% for the C6 position. EXAMPLE 21: Preparation of 6-O-Methanesulfonylhyaluronic acid (HA-Ms) 20 To a solution of 500mg (0.806mmol) of TBA salt of HA (MW 20,000) in 20 ml of N-methyl-2-pyrrolidone were added 829pL (4.84mmol) of DIEA by stirring under nitrogen. MsCI (188pL; 2.42mmol) was then added dropwise at room temperature, whereupon a yellow solution was formed. After 1 h stirring at room temperature, the reaction mixture was quenched by adding saturated NaHCO 3 solution (40ml) 25 and bringing the total volume to 100ml with water (resulting pH: 9.5); stirring was maintained overnight. The resulting solution was ultrafiltered and concentrated in a rotary evaporator. The solution was freeze-dried to afford 310mg of a white solid. Total mesylate DS 50% mol/mol by proton NMR, primary mesylates 31% mol/mol by carbon NMR, selectivity 62% for the C6 position. 30 EXAMPLE 22: Preparation of 6-O-Methanesulfonylhyaluronic acid (HA-Ms) To a solution of 500mg (0.806mmol) of TBA salt of HA (MW 20,000) in 20 ml of N-methyl-2-pyrrolidone were added 829pL (4.84mmol) of DIEA by stirring under WO 2007/085629 PCT/EP2007/050726 19 nitrogen at -10oC. MsCI (188pL; 2.42mmol) was then added dropwise and the resulting mixture was stirred for lh at -10oC. The reaction mixture was quenched by adding saturated NaHCO 3 solution (40ml) and bringing the total volume to 100ml with water (resulting pH: 9.5); stirring was maintained overnight. The 5 resulting solution was ultrafiltered and concentrated in a rotary evaporator. The solution was freeze-dried to afford 250mg of a white solid. Total mesylate DS 41% mol/mol by proton NMR, primary mesylates 39% mol/mol by carbon NMR, selectivity 95% for the C6 position. An HSQC NMR spectrum confirmed the selectivity. 10 EXAMPLE 23: Preparation of 6-O-Methanesulfonylhyaluronic acid (HA-Ms) To a solution of 500mg (0.806mmol) of TBA salt of HA (MW 20,000) in 20 ml of N-methyl-2-pyrrolidone were added 829pL (4.84mmol) of DIEA by stirring under nitrogen at 0oC. MsCI (188pL; 2.42mmol) was then added dropwise and the resulting mixture was stirred for 1 h at 0oC. The reaction mixture was quenched by 15 adding saturated NaHCO 3 solution (40ml) and bringing the total volume to 100ml with water (resulting pH: 9.5); stirring was maintained overnight. The resulting solution was ultrafiltered and concentrated in a rotary evaporator. The solution was freeze-dried to afford 275 mg of white solid. Total mesylate DS 44% mol/mol by proton NMR, primary mesylates 40% mol/mol by carbon NMR, selectivity 90% for 20 the C6 position. EXAMPLE 24: Preparation of 6-O-Methotrexylhyaluronic acid A solution of HA-OMs:TBA salt from Example 10 (500mg; 0.73mmol) in DMSO (15 ml) was treated with a solution of methotrexate (833mg; 1.83mmol) in DMSO (10 ml) in the presence of solid cesium carbonate (596mg; 1.83mmol). The mixture 25 was stirred under nitrogen at 800C for 18h, whereupon it darkened with formation of solids. It was then cooled to ambient temperature, poured into 100ml of water (pH 6.5), treated with 15ml of saturated NaCI solution, and stirred for 1.5h. Then solids were filtered off and the solution was ultrafiltered, concentrated and freeze dried to give 131 mg of a yellow-brownish solid. DS of MTX by NMR: 40% mol/mol; 30 13C NMR shows that 40% of C6 is modified. HPLC analysis gave 32% w/w, corresponding to 40% mol/mol. In addition, the NMR revealed the absence of any residual secondary mesylate group and that the basic structure of HA was WO 2007/085629 PCT/EP2007/050726 20 unchanged, except some of the C-6 position because of the substitution by MTX. This demonstrates that any possible leaving (mesylate) groups introduced at the secondary positions (C-4,C-2',C-3') during the mesylation reaction have been hydrolysed during the displacement reaction under the basic conditions either 5 directly or by way of 2',3'-anhydride formation followed by hydrolysis with the retention of configuration at those positions. The NMR spectrum was repeated on the same sample after 3-months storage at room temperature, it provides the same peaks and the same intensity as those obtained on the freshly prepared product, thus indicating that the substitution degree is maintained and no by 10 products are formed. EXAMPLE 25 Preparation of HA-Cl: TBA salt. 50g of hyaluronan sodium salt were suspended in 900 mL of dry dimethylformamide under nitrogen, with mechanical stirring at 200C. The suspension was then cooled to -10OC and 97 mL of methanesulfonyl chloride were 15 added during 30min. After additional 30min at -10oC, the temperature was raised to 200C. After l1h the temperature was gradually raised (during lh) to 600C and stirring was continued for 18h. The reaction mixture was then poured in portions into a mixture of ice and sodium carbonate solution (4 L, initial pH=11) with vigorous mixing, maintaining the pH around 9 by addition of 1.5 M NaOH when 20 required. The resulting brownish suspension (final volume 6 L) was stirred at pH 9.5 at room temperature for about 48h, whereupon a clear solution formed. This was filtered to remove solids and then ultrafiltered (10 KDa cut-off membrane). The resulting solution was concentrated in a rotary evaporator to a final volume of about 1 litre and treated with amberlite IRA-120 loaded with TBA. Then it was 25 freeze-dried to afford 46.7g of HA-6-Cl: TBA salt as an off-white solid (DS 64% mol/mol, determined by 13C NMR). EXAMPLE 26 : Preparation of HA-lbuprofen HA-Ms:TBA salt (400mg; 0.64mmol) as prepared in example 12 and ibuprofen (333mg; 1.61mmol) were dissolved in DMSO (16ml) by stirring under nitrogen at 30 room temperature. Solid cesium carbonate (264mg; 0.81 mmol) was added and the suspension was heated at 700C for 20h with stirring. The resulting yellow-orange solution was poured into 150ml of water (pH was 6.5) and 10ml of saturated NaCI WO 2007/085629 PCT/EP2007/050726 21 solution were added. After stirring for 30min, the solution was ultrafiltered, concentrated and freeze-dried to give 0.15g of a white solid. DS by proton NMR: 27% mol/mol. EXAMPLE 27 : Preparation of HA-lbuprofen 5 HA-CI:TBA salt (1g; 1.6mmol) as prepared in example 25 and ibuprofen (670mg; 3.2mmol) were dissolved in DMSO (50ml) by stirring under nitrogen at room temperature. Solid cesium carbonate (264mg; 0.81mmol) was added and the suspension was heated at 800C for 40h with stirring. The resulting dark yellow solution was poured into 100ml of water (pH was 8) and then ultrafiltered, 10 concentrated and freeze-dried to give g of a light brown solid. DS by proton NMR: 20% mol/mol. EXAMPLE 28: Preparation of HA-Penicillin G A solution of HA-Ms:TBA salt (400mg; 0.64mmol) as prepared in example 12, 18 crown-6 (338 mg; 1.28mmol) and Penicillin G sodium salt (574mg; 1.61mmol) in 15 DMSO (16ml) was heated at 70oC for 20h with stirring. The resulting yellow solution was poured into 150ml of water (pH was 6.5) and 10ml of saturated NaCI solution were added. After stirring for 30min, the solution was ultrafiltered, concentrated and freeze-dried to give 0.29g of a white solid. DS by proton NMR: 26% mol/mol. 20 EXAMPLE 29: Preparation of HA-Penicillin G HA-Cl:TBA salt (1g; 1.6mmol) as prepared in example 25, 18-crown-6 (840 mg; 3.2mmol) and Penicillin G sodium salt (1.13g; 3.2mmol) were dissolved in DMSO (50ml) by stirring at room temperature. The solution was heated at 800C for 40h with stirring, then it was poured into 100ml of water (pH was 7.4) and ultrafiltered, 25 concentrated and freeze-dried to give 1 g (yield 64%) of a pale yellow solid. DS by proton NMR: 6% mol/mol. EXAMPLE 30: Preparation of HA-Albumin HA-CI:TBA salt (1g; 1.6mmol) as prepared in example 25 and Human serum Albumin (300mg) were dissolved in DMSO (50ml) by stirring under nitrogen at 30 room temperature. Solid cesium carbonate (264mg; 0.81 mmol) was added and the suspension was heated at 800C for 40h with stirring. The resulting brown solution WO 2007/085629 PCT/EP2007/050726 22 was poured into 100ml of water (pH was 9.5) and then ultrafiltered, concentrated and freeze-dried to give 0.9 g of a light brown solid. DS by HPLC RP: 5% mol/mol. EXAMPLE 31: Preparation of 6-O-Methotrexylhyaluronic acid HA:TBA salt (250mg; 0.403mmol; MW 20,000) was dissolved in DMSO (10ml) by 5 stirring and gentle heating under nitrogen; triethylamine (452pL; 3.22mmol) was then added at room temperature followed by dropwise addition of MsCI (157pL; 2.02mmol), whereupon a yellow solution formed. After l1h stirring at room temperature, further 0.50ml of triethylamine were added, the reaction flask was connected to the vacuum and gently heated up to 500 C (bath temperature), until 10 gas evolution ceased. Then 1.10g (2.43mmol) of methotrexate and 792mg (2.43mmol) of cesium carbonate were added and the mixture was stirred at 800 C overnight. Half of the reaction mixture was quenched by pouring into water (20ml); pH 6.3. The pH was adjusted to 6.8 with saturated NaHCO 3 solution and then 10ml of saturated NaCI solution were added. After stirring for 10min, the solution 15 was ultrafiltered, concentrated in a rotary evaporator and freeze-dried to give 60mg of a yellow solid. The DS of MTX was found to be 11.6% w/w by HPLC and was confirmed by NMR analysis (12% mol/mol), which also showed a small percentage of left mesylates on the polymer. The rest of the reaction mixture was worked up after further 24h at 800 C (40h 20 overall) as described above, to afford 103mg of a yellow solid. DS in MTX 14.4% w/w by HPLC, confirmed by NMR analysis (15% mol/mol), which did not show any mesylate left on the polymer. MW 269610, PI 10.5. Cross-linking ester bonds were cleaved by hydrolyzing the freeze dried product in 10ml of a carbonate buffer (pH 10) for 8h. After neutralization and dialysis, freeze-drying afforded 96 mg of a 25 yellow solid. The DS of MTX in the product was 12.6% w/w by HPLC, which was confirmed by NMR analysis (13% mol/mol); MW 27,120, PI 1.9. EXAMPLE 32: Preparation of 6-O-methotrexylhyaluronic acid To a solution of HATBA (50g, Mw 70,000) in 1000 ml of dry DMF under stirring, mesylchloride (10 eq) was added dropwise in 1 hr time at -10oC under N 2 flow. 30 The mixture was maintained for 1 hour at room temperature and then heated at 600C for 16 hr. The work-up allow the obtainment of 46.9 g of HA-CL having chlorine content 4.2% w/w ( 13

C-NMR).

WO 2007/085629 PCT/EP2007/050726 23 A solution of the HA-CI TBA salt (20 g) in DMSO (1.25 L) is treated with MTX (29.3g) and cesium carbonate (21 g) at 800C for 40 h, giving 5.6 g of a yellow solid. 13 C-NMR spectrum confirmed the occurrence of the linkage in position 6 of N 5 acetyl-D-glucosamine: the peak at 64 ppm is assigned at CH 2 0-MTX and its intensity corresponds to the decrease of the peak at 44 ppm (CH 2 CI0) compared to the parent chlorine derivative. The MTX content was 18.8% w/w (HPLC); free MTX was 0.1% w/w, water content: 8.2% w/w; MW: 11.000; PI: 1.4. In addition, the NMR reveals the presence of residual chlorine which amounts to 1.76% w/w. 10 EXAMPLE 33: Preparation of 6-O-Methanesulfonylhyaluronic acid TBA salt (HA-Ms:TBA) To a solution of 5.0g (8.1 mmol) of HA:TBA (MW 5,000) in 100 mL of dry DMF were added 3.1 mL of DIEA (5.62 mL, 33.9 mmol) under stirring and N 2 flow at -10oC. MsCI (1.25 mL; 16.1 mmol) was then added dropwise and the resulting 15 mixture was stirred for 1 h at -10oC. The reaction mixture was quenched by adding saturated Na 2

CO

3 solution (200mL) and bringing the total volume to 1L with water; pH was adjusted to 10.5 with dilute HCI solution and stirring was maintained overnight. The resulting solution was ultrafiltered and concentrated in a rotary evaporator. A small portion was freeze-dried (100mg) for NMR analysis: primary 20 mesylates 30% mol/mol by NMR, selectivity 100% for C6. (3.2 g; Mw: 6,925; P.I. 1.87) EXAMPLE 34: Preparation of 6-O-Methanesulfonylhyaluronic acid TBA salt (HA-Ms:TBA) To a solution of 10.0g (16.1mmol) of TBA salt of HA (MW 20,000) in 250 ml of 25 DMF were added 7.58ml (44.3mmol) of DIEA by stirring under nitrogen at -10oC. MsCI (1.56mL; 20.1 mmol) was then added dropwise and the resulting mixture was stirred for l1h at -10oC. The reaction mixture was quenched by adding saturated Na 2

CO

3 solution (400mL) and bringing the total volume to 2L with water; pH was adjuasted to 10.5 with dilute HCI solution and stirring was maintained overnight. 30 The resulting solution was ultrafiltered and concentrated in a rotary evaporator. A small portion was freeze-dried (100mg) for NMR analysis: primary mesylates 24% mol/mol by NMR, selectivity 100% for C6.

WO 2007/085629 PCT/EP2007/050726 24 The rest of the solution was treated with amberlite IRA-120 loaded with TBA and freeze-dried to afford 9.92g of a white solid (HA-Ms:TBA salt). EXAMPLE 35: Preparation of HA-Cl: sodium salt 5g of hyaluronan sodium salt (MW 200,000) were suspended in 90 mL of dry 5 dimethylformamide under nitrogen, with mechanical stirring at 200C. The suspension was then cooled to -10oC and 9.7 mL of methanesulfonyl chloride were added during 30min. After additional 30min at -10oC, the temperature was raised to 200C. After 1 h the temperature was gradually raised (during 1 h) to 600C and stirring was continued for 18h. The reaction mixture was then poured in 10 portions into a mixture of ice and sodium carbonate solution (400 mL, initial pH=11) with vigorous mixing, maintaining the pH around 9 by addition of 1.5 M NaOH when required. The resulting brownish suspension (final volume 500 mL) was stirred at pH 9.5 at room temperature for about 48h, whereupon a clear solution formed. This was filtered to remove solids and then ultrafiltered (10 KDa 15 cut-off membrane). The resulting solution was concentrated and freeze-dried to afford 4.05g of HA-6-CI: sodium salt as an off-white solid (DS 17% mol/mol, determined by 13C NMR). MW 79,560, P.I. 3.5. EXAMPLE 36: Preparation of HA-Cl: sodium salt 5g of hyaluronan sodium salt (MW 500,000) were suspended in 90 mL of dry 20 dimethylformamide under nitrogen, with mechanical stirring at 200C. The suspension was then cooled to -10oC and 9.7 mL of methanesulfonyl chloride were added during 30min. After additional 30min at -10oC, the temperature was raised to 200C. After 1 h the temperature was gradually raised (during 1 h) to 700C and stirring was continued for 21h. The reaction mixture was then poured in 25 portions into a mixture of ice and sodium carbonate solution (400 mL, initial pH=11) with vigorous mixing, maintaining the pH around 9 by addition of 1.5 M NaOH when required. The resulting brownish suspension (final volume 500 mL) was stirred at pH 9.5 at room temperature for about 48h, whereupon a clear solution formed. This was filtered to remove solids and then ultrafiltered (10 KDa 30 cut-off membrane). The resulting solution was concentrated and freeze-dried to afford 3.56g of HA-6-CI: sodium salt as an off-white solid (DS 10% mol/mol, determined by 13C NMR). MW 53,830, P.I. 4.02.

WO 2007/085629 PCT/EP2007/050726 25 EXAMPLE 37: Preparation of 6-O-Methanesulfonylhyaluronic acid TBA salt (HA-Ms:TBA) To a solution of 10.0g (16.1mmol) of TBA salt of HA (MW 180,000) in 500 ml of DMF were added 9.16ml (53.4mmol) of DIEA by stirring under nitrogen at -10oC. 5 MsCI (1.87mL; 24.2mmol) was then added dropwise and the resulting mixture was stirred for l1h at -10oC. The reaction mixture was quenched by adding saturated Na 2

CO

3 solution (400mL) and bringing the total volume to 2L with water; pH was adjuasted to 10.5 with dilute HCI solution and stirring was maintained overnight. The resulting solution was ultrafiltered and concentrated in a rotary evaporator. A lo small portion was freeze-dried (150mg) for NMR analysis: primary mesylates 30% mol/mol by NMR, selectivity 100% for C6. The rest of the solution was treated with amberlite IRA-120 loaded with TBA and freeze-dried to afford 9.80g of a white solid (HA-Ms:TBA salt). EXAMPLE 38: Preparation of 6-O-Methanesulfonylhyaluronic acid TBA salt 15 (HA-Ms:TBA) To a solution of 20.0g (32.2mmol) of TBA salt of HA (MW 180,000) in 1000 ml of DMF were added 36.7ml (214mmol) of DIEA by stirring under nitrogen at -100C. MsCI (7.48mL; 97mmol) was then added dropwise and the resulting mixture was stirred for l1h at -10oC. The reaction mixture was quenched by adding saturated 20 Na 2

CO

3 solution (800mL) and bringing the total volume to 4L with water; pH was adjuasted to 10.5 with dilute HCI solution and stirring was maintained overnight. The resulting solution was ultrafiltered and concentrated in a rotary evaporator. A small portion was freeze-dried (120mg) for NMR analysis: primary mesylates 55% mol/mol by NMR, selectivity 100% for C6. 25 The rest of the solution was treated with amberlite IRA-120 loaded with TBA and freeze-dried to afford 19.95g of a white solid (HA-Ms:TBA salt). EXAMPLE 39: Preparation of 6-O-Methanesulfonylhyaluronic acid TBA salt (HA-Ms:TBA) To a solution of 2.00g (3.22mmol) of TBA salt of HA (MW 500,000) in 150 ml of 30 DMF were added 3.67ml (21.4mmol) of DIEA by stirring under nitrogen at -10oC. MsCI (750pL; 9.7mmol) was then added dropwise and the resulting mixture was stirred for l1h at -10oC. The reaction mixture was quenched by adding saturated WO 2007/085629 PCT/EP2007/050726 26 Na 2

CO

3 solution (80mL) and bringing the total volume to 1L with water; pH was adjuasted to 10.5 with dilute HCI solution and stirring was maintained overnight. The resulting solution was ultrafiltered and concentrated in a rotary evaporator. A small portion was freeze-dried (90mg) for NMR analysis: primary mesylates 70% 5 mol/mol by NMR, selectivity 100% for C6. The rest of the solution was treated with amberlite IRA-120 loaded with TBA and freeze-dried to afford 1.94g of a white solid (HA-Ms:TBA salt). EXAMPLE 40: Preparation of 6-O-Methotrexylhyaluronic acid A solution of HA-OMs:TBA salt from Example 34 (8.0g; 12.9mmol) in DMSO (250 10 ml) was treated with a solution of methotrexate (14.66g; 32.3mmol) in DMSO (150ml) in the presence of solid cesium carbonate (10.5g; 32.2mmol). The mixture was stirred under nitrogen at 800C for 20h. It was then cooled to ambient temperature and poured into a carbonate buffer, adjusting the pH to 9.7 and the volume to 2L. After stirring for 18h the solution was neutralized, filtered, 15 ultrafiltered, concentrated and freeze-dried to give 4.70g of a yellow solid. DS of MTX by NMR: 7.5% mol/mol; MW 27,960, P.I. 1.92. EXAMPLE 41: Preparation of 6-O-Methotrexylhyaluronic acid A solution of HA-OMs:TBA salt from Example 37 (7.0g; 11.3mmol) in DMSO (670 ml) was treated with a solution of methotrexate (12.79g; 28.1mmol) in DMSO 20 (120ml) in the presence of solid cesium carbonate (9.15g; 28.1mmol). The mixture was stirred under nitrogen at 750C for 18h. It was then cooled to ambient temperature and poured into a carbonate buffer, adjusting the pH to 8.8 and the volume to 2.5L. After stirring for 24h the solution was neutralized, filtered, ultrafiltered, concentrated and freeze-dried to give 4.30g of a yellow solid. DS of 25 MTX by NMR: 13% mol/mol; MW 208,400, P.I. 2.18. EXAMPLE 42: Preparation of 6-O-Methotrexylhyaluronic acid A solution of HA-OMs:TBA salt from Example 38 (13.2g; 21.3mmol) in DMSO (1270 ml) was treated with a solution of methotrexate (24.13g; 53.1mmol) in DMSO (120ml) in the presence of solid cesium carbonate (17.26g; 53.1mmol). 30 The mixture was stirred under nitrogen at 750C for 18h. It was then cooled to ambient temperature and poured into a carbonate buffer, adjusting the pH to 10.0 and the volume to 5L. After stirring for 18h the solution was neutralized, filtered, WO 2007/085629 PCT/EP2007/050726 27 ultrafiltered, concentrated and freeze-dried to give 6.52g of a yellow solid. DS of MTX by NMR: 20% mol/mol; MW 217,300, P.I. 2.02. EXAMPLE 43: Preparation of 6-O-Methotrexylhyaluronic acid A solution of HA-OMs:TBA salt from Example 39 (500mg; 0.74mmol) in DMSO 5 (80ml) was treated with a solution of methotrexate (1.01g; 2.23mmol) in DMSO (1Oml) in the presence of solid cesium carbonate (726mg; 2.23mmol). The mixture was stirred under nitrogen at 800C for 22h. It was then cooled to ambient temperature and poured into a carbonate buffer, adjusting the pH to 10.0 and the volume to 400mL. After stirring for 18h the solution was neutralized, filtered, 10 ultrafiltered, concentrated and freeze-dried to give 260mg of a yellow solid. DS of MTX by NMR: 11% mol/mol; MW 460,100, P.I. 2.21. EXAMPLE 44: Preparation of 6-O-Methotrexylhyaluronic acid A solution of HA-OMs sodium salt from Example 33 (1.0g; 2.0 mmol) in DMSO (40 ml) was treated with a solution of methotrexate (1.83 g; 4mmol) in DMSO (40ml) in 15 the presence of solid cesium carbonate (1.30; 2mmol). The mixture was stirred under nitrogen at 800C for 20h. The solution was neutralized using Na 2 CO3 saturated solution bringing the final volume to 500 mL, filtered, ultrafiltered, concentrated and freeze-dried to give 500 mg of a yellow solid. DS of MTX by HPLC: 7.8% w/w; MW 16,000, P.I. 2.4. 20 EXAMPLE 45 : Preparation of HA-lbuprofen HA-Ms:TBA salt (500mg; 0.80mmol) as prepared in example 20 and ibuprofen (416mg; 2.01mmol) were dissolved in DMSO (20ml) by stirring under nitrogen at room temperature. Solid cesium carbonate (330mg; 1.01 mmol) was added and the suspension was heated at 700C for 20h with stirring. The resulting solution was 25 poured into 200ml of water (pH was 6.5) and 10 ml of saturated NaCI solution were added. After stirring for 30min, the solution was ultrafiltered, concentrated and freeze-dried to give 0.22g of a white solid. DS by proton NMR: 30% mol/mol. EXAMPLE 46 : Preparation of HA-Naproxen HA-Ms:TBA salt (500mg; 0.80mmol) as prepared in example 20 and naproxen 30 (463mg; 2.01mmol) were dissolved in DMSO (20ml) by stirring under nitrogen at room temperature. Solid cesium carbonate (330mg; 1.01 mmol) was added and the suspension was heated at 700C for 20h with stirring. The resulting solution was WO 2007/085629 PCT/EP2007/050726 28 poured into 200ml of water (pH was 6.6) and 10 ml of saturated NaCI solution were added. After stirring for 30min, the solution was ultrafiltered, concentrated and freeze-dried to give 0.27g of a white solid. DS by proton NMR: 28% mol/mol. EXAMPLE 47: Preparation of HA-Lisinopril 5 HA-Ms:TBA salt (500mg; 0.80mmol) as prepared in example 20 and lisinopril (887mg; 2.01mmol) were dissolved in DMSO (25ml) by stirring under nitrogen at room temperature. Solid cesium carbonate (655mg; 2.01 mmol) was added and the suspension was heated at 700C for 20h with stirring. The resulting solution was poured into 200ml of water (pH was 6.5) and 10 ml of saturated NaCI solution were 1o added. After stirring for 30min, the mixture was filtered, ultrafiltered, concentrated and freeze-dried to give 0.20g of a white solid. DS by proton NMR: 26% mol/mol. EXAMPLE 48 : Preparation of HA-Nalidixate HA-Ms:TBA salt (500mg; 0.80mmol) as prepared in example 20 and nalidixic acid (467mg; 2.01mmol) were dissolved in DMSO (20ml) by stirring under nitrogen at 15 room temperature. Solid cesium carbonate (330mg; 1.01 mmol) was added and the suspension was heated at 700C for 20h with stirring. The resulting solution was poured into 200ml of water (pH was 6.6) and 10 ml of saturated NaCI solution were added. After stirring for 30min, the solution was ultrafiltered, concentrated and freeze-dried to give 0.26g of a white solid. DS by proton NMR: 30% mol/mol. 20 EXAMPLE 49: Preparation of HA-Penicillin G A solution of HA-Ms:TBA salt (400mg; 0.64mmol) as prepared in example 20, 18 crown-6 (338 mg; 1.28mmol) and Penicillin G sodium salt (574mg; 1.61mmol) in DMSO (16ml) was heated at 70oC for 20h with stirring. The resulting yellow solution was poured into 150ml of water (pH was 6.5) and 25 10ml of saturated NaCI solution were added. After stirring for 30min, the solution was ultrafiltered, concentrated and freeze-dried to give 0.27g of a white solid. DS by proton NMR: 31% mol/mol. EXAMPLE 50: Preparation of HA-Cefazolin A solution of HA-Ms:TBA salt (400mg; 0.64mmol) as prepared in example 20, 18 30 crown-6 (338 mg; 1.28mmol) and cefazolin sodium salt (767mg; 1.61mmol) in DMSO (18ml) was heated at 70oC for 20h with stirring.

WO 2007/085629 PCT/EP2007/050726 29 The resulting solution was poured into 180ml of water (pH was 6.7) and 10ml of saturated NaCI solution were added. After stirring for 30min, the solution was ultrafiltered, concentrated and freeze-dried to give 0.25g of a white solid. DS by proton NMR: 29% mol/mol.

Claims

1-3 heteroatoms selected in the group consisting of nitrogen, sulphur and oxygen; 15 Ar represents: 1,4-phenyl group, 1,4-phenyl group condensed with one or more 5 6 membered aromatic rings, 1,4-phenyl group condensed with one or more 5-6 membered heterocycles, wherein said Ar is possibly substituted with R 2 ; rings A and b, independently from one another, may be aromatic or non-aromatic. 20 2) DDS of claim 1 wherein the linkage between the hyaluronic acid and the active agent is an ester, an amino, an ether, a thioether, an amide, preferably an ester. 3) DDS of claims 1-2 wherein the therapeutic active agent is chosen from 25 drugs belonging to a number of different therapeutic categories: analgesic, WO 2007/085629 PCT/EP2007/050726 31 antihypertensive, anestetic, diuretic, bronchodilator, calcium channel blocker, cholinergic, CNS agent, estrogen, immunomodulator, immunosuppressant, lipotropic, anxiolytic, antiulcerative, antiarrhytmic, antianginal, antibiotic, anti inflammatory, antiviral, thrombolitic, vasodilator, antipyretic, antidepressant, 5 antipsychotic, antitumour, mucolytic, narcotic antagonist, hormones, anticonvulsant, antihistaminic, antifungal, antipsoriatic. (preferably anti inflammatory, antibiotic, antitumor) 4) DDS of claims 1-3 wherein the active agent is present in amount comprised 10 between 0.1 and 60% w/w with respect to the total weight of the DDS (preferably 1 and 50%) 5) DDS of claims 1-4 wherein the secondary hydroxyl groups of the hyaluronic acid are derivatised to form a group selected from: -OR, -OCOR, -SO 2 H, -OPO 3 H 2 , 15 -O-CO-(CH 2 )n-COOH, -O-(CH 2 )n-OCOR, wherein n is 1-4 and R is C1-C10 alkyl, NH 2 , -NHCOCH 3 6) DDS of claims 1- 5 either in the acid form or salified with alkaline metals or with earth-alkaline metals or with transition metals 20 7) Use of drug delivery systems of claims 1-6 in the manufacture of a medicament 8) Pharmaceutical compositions containing the drug delivery systems of 25 claims 1-6 in admixture with pharmaceutically acceptable excipients and/or diluents 9) Pharmaceutical composition of claim 8 in injectable form 30 10) Process for the preparation of the drug delivery system of claims 1-6, which comprises the following reaction steps: WO 2007/085629 PCT/EP2007/050726 32 (a) introducing a leaving group at the C-6 position of the N-acetyl-D-glucosamine units of the hyaluronic acid either in the free form or in the salt form thus obtaining a HA-6-activated (b) forming a chemical linkage between the C6 position of the HA-6-activated and 5 the therapeutic active agent by displacing the leaving group (at the C6 position of HA) with a nucleophilic group present on the therapeutic active agent, thereby obtaining a HA-6-active agent (c) possible displacing of any un-substituted leaving group from the HA-6-active agent obtained in step (b) 10 (d) recovering the HA-6-active agent 11) Process of claim 10 wherein the HA-6-activated obtained from step (a) is isolated from the reaction mixture and then reacted with the therapeutic active agent according to step (b) 15 12) Process of claim 10 wherein the step (b) is performed directly on the reaction mixture of step (a) containing the HA-6-activated 13) Process of claims 10-12 wherein the leaving group introduced at the C-6 20 position of the N-acetyl-D-glucosamine units of the hyaluronic acid is selected from the group consisting of sulfonate group, phosphonate group (triphenylphoshonate), cyanide (CN-), nitrite (N02-), halogen (preferably chloro), sulphate group, halogensulfate group, nitrate, halogensulfite (chlorosulfite) 25 14) Process for the preparation of a drug delivery system of claims 1-6, which comprises the following reaction steps: (a) introducing a sulfonate group at the C-6 position of the N-acetyl-D-glucosamine units of the hyaluronic acid in the salt form thus obtaining a HA-6-sulfonated (b) forming a chemical linkage between the C6 position of the HA-6-sulfonated and 30 the therapeutic active agent by displacing the sulfonated group at the C6 position of HA with the nucleophilic group present on a therapeutic active agent, thereby obtaining a HA-6-active agent WO 2007/085629 PCT/EP2007/050726 33 (c) recovering the HA-6-active agent 15) Process of claim 14 wherein the linkage between the hyaluronic acid and the active agent is an ester, an amino, an ether, a thioether, an amide. 5 16) Process of claim 15 wherein the linkage between the hyaluronic acid and the active agent is an ester 17) Process of claims 14-16 wherein the reagent used for introducing the lo sulfonate group is an alkyl- or aryl-sulfonyl halide, preferably chloride, in presence of an organic or inorganic base, preferably organic base. 18) Process of claim 17 wherein the reagent is methylsulfonyl chloride or toluene-p-sulfonyl chloride and the organic base is diisopropylethylamine or triethylamine. 15 19) Drug delivery system consisting of hyaluronic acid and a compound of formula (I), whereby the carboxylic group of compound of formula (I) is covalently linked at the C-6 position of the N-acetyl-D-glucosamine residue of the hyaluronic acid by means of an ester linkage -COOH N1 I N ( ,- CH 2 - Ar- CONH- CH- (CH 2 ) 2 - 7 COOH R2 formula (I) 20 and whereby said DDS is obtained by a process which comprises the following reaction steps: WO 2007/085629 PCT/EP2007/050726 34 (a) introducing at the C-6 position of the N-acetyl-D-glucosamine units of the hyaluronic acid either in the free form or in the salt form a leaving group selected from the group consisting of sulfonate group, phosphonate group (triphenylphoshonate), cyanide (CN-), nitrite (N02-), sulphate group, 5 halogensulfate group (preferably chloro sulphate), nitrate, halogensulfite (chlorosulfite) thus obtaining a HA-6-activated (b) forming an ester linkage between the C6 position of the HA-6-activated and the compound of formula (I) by displacing the leaving group (at the C6 position of HA) with a carboxylic group present on compound (I), thereby obtaining a HA-6 10 compound of formula (I) (c) recovering the HA-6-compound of formula (I) 20) DDS of claim 19, having a C6-DSw comprised between 1 and 50%, preferably between 5 and 40%. 15 21) DDS of claim 19-20 wherein the compound of formula (I) is methotrexate. 22) DDS of claim 19-21 wherein the HA-6-activated obtained from step (a) is isolated from the reaction mixture and then reacted with the therapeutic active 20 agent according to step (b). 23) DDS of claim 19-22 wherein the step (b) is performed directly on the reaction mixture of step (a) containing the HA-6-activated. 25 24) DDS of claims 19-23 wherein the reagent used for introducing the sulfonate group is an alkyl- or aryl-sulfonyl halide, preferably chloride, in presence of an organic or inorganic base, preferably organic base. 25) DDS of claim 24 wherein the reagent is methylsulfonyl chloride or toluene-p 30 sulfonyl chloride and the organic base is diisopropylethylamine or triethylamine. WO 2007/085629 PCT/EP2007/050726 35 26) Use of DDS of claims 19-25 in the manufacture of a medicament. 27) Pharmaceutical compositions containing the drug delivery systems of claims

19-25 in admixture with pharmaceutically acceptable excipients and/or diluents. 5 28) Pharmaceutical composition of claim 27 in injectable form. 29) HA-6-activated obtainable by introducing, at the C-6 position of the N-acetyl D-glucosamine units of hyaluronic acid either in the free form or in the salt form, a 10 leaving group selected from the group consisting of sulfonate group, phosphonate group (triphenylphoshonate), cyanide (CN-), nitrite (NO2-), sulphate group, halogensulfate group (preferably chloro sulphate), nitrate, halogensulfite (chlorosulfite). 15 30) HA-6-activated of claim 29, wherein the leaving group is sulphonate group. 31) HA-6-activated of claims 29-30, having a C6-DSmoI comprised between 10 and 91%. 20 32) HA-6-activated of claim 29-30, having a C6-DSmoI comprised between 20 and 90%. 33) HA-6-activated of claims 29-30, having a C6-DSmoI comprised between 40 and 80%.